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Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/8556

Title: Dorsal unpaired median neurons of Locusta migratoria express ivermectin- and fipronil-sensitive glutamate-gated chloride channels
Authors: JANSSEN, Daniel
Derst, Christian
BUCKINX, Roeland
RIGO, Jean-Michel
Issue Date: 2007
Citation: JOURNAL OF NEUROPHYSIOLOGY, 97(4). p. 2642-2650
Abstract: Together with type A GABA and strychnine-sensitive glycine receptors, glutamate-gated chloride channels ( GluCl) are members of the Cys-loop family of ionotropic receptors, which mediate fast inhibitory neurotransmission. To date, GluCls are found in invertebrates only and therefore represent potential specific targets for insecticides, such as ivermectin and fipronil. In this study, we identified the functional expression of GluCls in dorsal unpaired median ( DUM) neurons of the metathoracic ganglion of Locusta migratoria using electrophysiological and molecular biological techniques. In whole cell patch-clamped DUM neurons, glutamate-induced changes in both their membrane potentials (current-clamp) and currents (voltage-clamp) were dependent on the chloride equilibrium potential. On continuous application of glutamate, the glutamate-elicited current response became rapidly and completely desensitized. Application of glutamate in the presence of 10 mu M fipronil or 100 mu M picrotoxin reversibly decreased GluCl-mediated currents by 87 and 39%, respectively. Furthermore, 1 mu M ivermectin induced a persistent chloride current, suggesting the expression of ivermectin-sensitive GluCl alpha subunits. A degenerate PCR/RACE strategy was used to clone the full-length L. migratoria LmGlC1 alpha subunit. Finally, RT-PCR experiments demonstrated the presence of LmGluC1 alpha transcripts in locust DUM neurons. Our results provide the first direct evidence of a functional ivermectin-sensitive GluCl channel on the cell surface of DUM neurons of L. migratoria.
Notes: daniel.janssen@uhasselt.be
URI: http://hdl.handle.net/1942/8556
DOI: 10.1152/jn.01234.2006
ISI #: 000247929900008
ISSN: 0022-3077
Category: A1
Type: Journal Contribution
Appears in Collections: Research publications

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